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Pancreatic CancerPAC-MAINNCT04112836

Pancreatic Cancer Malnutrition and Pancreatic Exocrine Insufficiency in the Course of Chemotherapy in Unresectable Pancreatic Cancer

An observational study of Pancreatic Cancer and Exocrine Pancreatic Insufficiency, run by Moscow Clinical Scientific Center at 8 sites in 6 countries.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Malnutrition and cachexia are common in patients with advanced pancreatic ductal adenocarcinoma (PDAC) and have a significant influence on the tolerance and response to treatments. Read more about this study

Who is it for?
Ages 18 years and older
How many people
186 participants
Where
8 sitesin 6 countries
Study dates
15 Mar 2019to Aug 2020
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: patients with unresectable locally advanced or metastatic PDAC

Who may be able to join

  • age ≥ 18 years;
  • histological diagnosis of PDAC within one month from recruitment to the study;
  • radiological diagnosis of the advanced stage not suitable for upfront surgical resection (either locally advanced or metastatic) within 5 weeks from recruitment to the study;
  • data on the variables and the outcomes of interest are available;
  • a written consent to participate in the study;
  • being planned for chemotherapy;
  • no past history of anticancer treatment.

Who cannot join

  • poor performance status (Eastern Cooperative Oncology Group scale (ECOG) ≥ 3);
  • pregnancy;
  • surgery for PDAC in the past and developed progression.

Trial locations and contacts

8 sites in 6 countries.

Gabriele Capurso, MD, PhD contact

+39 02 26436548

capurso.gabriele@hsr.it

Enrique de Madaria, MD, PhD contact

madaria@hotmail.com

8 sites in 6 countries

Serbia2 sites, 2 recruiting
  • University Clinic "Dr. Dragisa Misovic-Dedinje"

    Belgrade

    Nikola Panic, MD, +381 11 3630600, nikola.panicmail@gmail.com

    Not yet recruiting
  • University of Belgrade

    Belgrade

    Nikola Panic, MD, +381 11 3630600, nikola.panicmail@gmail.com

    Not yet recruiting

Other trials in Serbia

Spain2 sites, 2 recruiting
  • Alicante University General Hospital

    Alicante

    Enrique de Madaria, MD, PhD, +34 965 933 468, madaria@hotmail.com

    Maryana Bozhychko, MD, +34 965 933 468, maryanabozhychko@gmail.com

    Not yet recruiting
  • University Hospital of Santiago de Compostela

    Santiago de Compostela

    Daniel de la Iglesia Garcia, MD, +34981951364, danieldelaiglesiagarcia@hotmail.com

    Not yet recruiting

Other trials in Spain

Italy1 site, 1 recruiting
  • IRCCS San Raffaele Scientific Institute

    Milan

    Gabriele Capurso, MD, PhD, +39 02 26436548, gabriele.capurso@gmail.com

    Recruiting

Other trials in Italy

Romania1 site, 1 recruiting
  • Clinical Emergency Hospital Bucharest

    Bucharest

    Vasile Sandru, MD, +0040728813095, drsandruvasile@gmail.com

    Recruiting

Other trials in Romania

Russia1 site, 1 recruiting
  • A.S. Loginov Moscow Clinical Scientific Center

    Moscow

    Mariia Kiriukova, MD, +7 495 303 15 57, kiryukovam@yandex.ru

    Recruiting

Other trials in Russia

Turkey (Türkiye)1 site, 1 recruiting
  • Istanbul University

    Istanbul

    Bartu Avci, +90 212 414 2000, bartuavci@ogr.iu.edu.tr

    Recruiting

Other trials in Turkey (Türkiye)

About this study

Malnutrition and cachexia are common in patients with advanced pancreatic ductal adenocarcinoma (PDAC) and have a significant influence on the tolerance and response to treatments. If timely identified, malnourished PDAC patients could be treated to increase their capacity to complete the planned treatments and therefore, possibly, improve their efficacy.

The aim of the study is to assess the impact of nutritional status, pancreatic exocrine insufficiency (PEI), and other clinical factors on patient outcomes in patients with advanced PDAC.

The nutritional status will be determined by means of Mini-Nutritional Assessment score and laboratory blood tests. PEI will be defined as the presence of typical symptoms and/or reduced fecal elastase. Analysis: chemotherapy dosing over the first 12 weeks of therapy (i.e. percent of chemotherapy received in the first 12 weeks, as defined above) PAC-MAIN will provide insights on the role of malnutrition and PEI in outcomes of PDAC.

Read the detailed description

Investigators hypothesize that malnutrition has an adverse impact on the clinical course of patients with advanced PDAC treated with chemotherapy.

Aims:

To investigate the association between the nutritional status and pancreatic exocrine function and the clinical outcomes of patients with advanced PDAC.

Study design:

The PAncreatic Cancer MAlnutrition and exocrine pancreatic INsufficiency in the course of chemotherapy in unresectable pancreatic cancer (PAC-MAIN) study is a non-profit, international, multicentre, prospective, observational, cohort study evaluating the effect of the nutritional status and pancreatic exocrine function on the main outcomes of patients with advanced PDAC. The study will be carried out in Russia, Turkey, Serbia, Romania, Italy, and Spain as a part of the Pancreas 2000 Educational Program. Pancreas 2000 is a post-graduate educational program that prepares young gastroenterologists, surgeons, radiologists, and other physicians for specialization in Pancreatology.

Patient-related:

  • sex, race, age at diagnosis
  • Mini-Nutritional Assessment (MNA) score
  • sarcopenia (measured with computed tomography (CT) fat free mass is reduced; i.e. appendicular\L2 skeletal muscle mass index <7.2 kg/m2 (men) or <5.5 kg/m2 (women));
  • cachexia (weight loss (WL)>5% in last 6 months, or WL>2% if body mass index (BMI) <20 kg/m² or sarcopenia);
  • 12-item functional assessment of anorexia/cachexia therapy anorexia/cachexia subscale (FAACT-A/CS-12)
  • a biliary stent
  • a duodenal stent
  • total and direct bilirubin
  • ECOG status
  • European Organization for Research and Treatment of Cancer (EORTC) QLQ-PAN26 scale
  • Date of diagnosis, visit 1, visit 2 (3 months), and death/loss from follow up
  • Check up on survival at 6m

Tumor-related:

  • Tumor site documented by endoscopic ultrasound, CT, or magnetic resonance imaging (head, body, or tail)
  • Stage according to the TNM classification
  • Vessels involved
  • Presence and site of metastatic disease
  • Ascites
  • CA-19-9
  • Response evaluation criteria in solid tumors (RECIST) (for visit 2)

Nutritional parameters:

  • Leucocytes (lymphocytes, neutrophils), neutrophil to lymphocytes ratio, erythrocytes, hemoglobin, hematocrit, platelets
  • C-reactive protein, total protein, albumin, cholesterol, iron, transferrin, ferritin, magnesium, zinc
  • International normalized ratio, activated partial thromboplastin time
  • Blood fasting glucose, glycated hemoglobin

Pancreatic function and treatment:

  • PEI, fecal elastase-1, pancreatic enzyme replacement therapy (PERT), date of starting PERT, the dosage of daily taken PERT
  • Diabetes mellitus (DM), date of DM diagnosis, DM type, DM treatment

Treatment-related:

  • Planned chemotherapy protocol Dosages of chemotherapy planned (mg/m2)
  • Percent of standard chemotherapy dose delivered
  • Percent of planned chemotherapy delivered
  • Changes to the predefined schedule (dose reduction, schedule modifications, stop before planned)
  • Date of treatment start and end
  • Adverse events (National Cancer Institute toxicity scale for visit 2)

Description of the intervention (schedule of visits):

Visit 1 (screening, within 1 month from initial diagnosis). Patients will be informed about the study. Once patients agree with the inclusion in the study the investigators will evaluate the inclusion and exclusion criteria. Those patients who meet all the inclusion criteria and none of the exclusion criteria will be finally included in the study. In this visit, patients, tumor-related variables, and general patients' features will be recorded, and quality of life questionnaire will be administered. The researcher will record weight, height, body mass index (BMI), unplanned WL % for the last 6 months.

Each patient's baseline nutrition status will be evaluated using the MNA scores prior to starting chemotherapy. Patients will be classified as in the group with no nutritional risk, at risk of malnutrition, or malnourished.

Nutritional parameters and pancreatic function will be evaluated through blood tests and a fecal test.

Visit 2 (3 months after the first dose of planned chemotherapy). The researcher will record in the case report form (CRF) the planned chemotherapy, schedule, doses, dose reduction, and any adverse event. The same variables recorded at Visit 1 will be checked again.

Check up 3 (end of the study, 6 months). The researcher will record in the CRF the overall survival and time until progression.

Medication of the study:

The study is of observational nature, so a pre-planned treatment is not considered. However, the use of pancreatic enzyme replacement treatment will be recorded as well as data regarding the employed chemotherapy regimen.

Power size calculation:

The expected percent of chemotherapy delivered in well-nourished patients was based on a study that assessed the chemotherapy dose intensity in gastrointestinal malignancies included pancreaticobiliary disease during the firsts 8 weeks after the start of the chemotherapy23. Based on an expected percentage of chemotherapy delivered of 70% in well-nourished patients, with a type I error of 0.05 and a type II error of 0.20, a sample size of 93 patients per group will be required in case of a percentage difference of chemotherapy delivered of 20% between well-nourished and malnourished, 163 patients per group in case of a difference of 15% between both groups and 356 patients per group in case of 10% of difference.

Discussion:

Given the sparse overall scientific data on the subject, the investigators have designed a study that addresses the impact of patient's nutritional status and dietary intervention on the clinical course of patients with advanced PDAC treated with chemotherapy and is aimed at establishing whether it affects both tolerance and tumor response to medical therapy. PAC-MAIN will be the first study specifically investigating whether the nutritional status influences the possibility to complete planned chemotherapy in patients with advanced PDAC.

Keywords
pancreatic cancer, locally advanced, metastatic, nutritional status, exocrine pancreatic insufficiency, chemotherapy, dose-intensity
Medical subject headings
Pancreatic Neoplasms, Exocrine Pancreatic Insufficiency, Malnutrition, Neoplasm Metastasis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT04112836
Study groupRoleWhat they receive
Normal nutritional statusPatients, fulfilled inclusion criteria with Mini-Nutritional Assessment score of 24-30 points.
MalnourishedPatients, fulfilled inclusion criteria with Mini-Nutritional Assessment score of fewer than 17 points.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Percent of standard chemotherapy dose delivered

    Drug doses will be expressed in weight-based, body surface area (BSA)-based, Area Under the Curve (AUC) units or flat dose, according to standard dosing practice for a given drug or combination. For each drug in a regimen, the sum of the doses delivered during the first 12 weeks of therapy will be divided by the sum of the expected doses based on published standard schedule and dosing. The mean percent dose delivered of all drugs in a regimen will be reported as 'percent of standard chemotherapy dose delivered.' The investigators will use percent of standard chemotherapy dose delivered to estimate the overall relative dose delivered.

    Measured: 12 weeks after the diagnosis

  2. Percent of planned chemotherapy delivered

    Similarly, the sum of the doses delivered during the first 12 weeks of therapy will be divided by the sum of the expected doses based on each patient's starting chemotherapy dose, and the mean percent dose delivered for all drugs in a regimen will be reported as 'percent of planned chemotherapy delivered.' The investigators will use percent of planned chemotherapy dose delivered to quantify further dose reductions from starting dose and as an indicator of overall toxicity.

    Measured: 12 weeks after the diagnosis

Secondary outcomes (6)
  1. Percent of patients with chemotherapy-related toxicity in each group

    Measured: 12 weeks after the diagnosis

  2. Survival at 6 months

    Measured: 12 weeks after the diagnosis, 6 months

  3. Progression-free survival

    Measured: 6 months

  4. Quality of Life (EORTC) QLQ-PAN26 scale

    The pancreatic cancer module is designed for patients at all disease stages undergoing surgical resection, palliative surgical intervention, endoscopic palliation or palliative chemotherapy (Fitzsimmons et al., 1999a,b). The module comprises 26 questions assessing pain, dietary changes, jaundice, altered bowel habit, emotional problems related to pancreatic cancer, and other symptoms (cachexia, indigestion, flatulence, dry mouth, taste changes). The answers range is the following: not at all - 1 point, a little - 2 points, quite a bit - 3 points, very much - 4 points. Minimum score is 26, maximum is 106. The higher total score represents the worse quality of life.

    Measured: 12 weeks after the diagnosis

  5. Number of hospitalizations

    Measured: 12 weeks after the diagnosis

  6. Factors associated with the percent of chemotherapy received

    Measured: 12 weeks after the diagnosis

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Oct 2019
  2. Study start15 Mar 2019
  3. Primary completionJun 2020 (estimated)
  4. Study completionAug 2020 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
186 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04112836
Sponsor's protocol ID
2/2019
Acronym
PAC-MAIN
Status last verified
Oct 2019
First submitted
30 Sep 2019
Last updated
16 Oct 2019
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Publications

  • Kiriukova M, de la Iglesia Garcia D, Panic N, Bozhychko M, Avci B, Maisonneuve P, de-Madaria E, Capurso G, Sandru V. Pancreatic Cancer Malnutrition and Pancreatic Exocrine Insufficiency in the Course of Chemotherapy in Unresectable Pancreatic Cancer. Front Med (Lausanne). 2020 Sep 3;7:495. doi: 10.3389/fmed.2020.00495. eCollection 2020.

    PubMed 33015088

Questions about this trial

What is this clinical trial studying?

An observational study of Pancreatic Cancer and Exocrine Pancreatic Insufficiency, run by Moscow Clinical Scientific Center at 8 sites in 6 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 16 Oct 2019. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 8 sites in Serbia, Spain, Italy, Romania, Russia and 1 more country. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Gabriele Capurso, MD, PhD (+39 02 26436548, capurso.gabriele@hsr.it), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Percent of standard chemotherapy dose delivered (time frame: 12 weeks after the diagnosis). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04112836, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Oct 2019.

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